Struggling through Chemo
Hi all, My nurse has just introduced me to this group. I’m hoping to connect and share my story and hopefully somehow feel better. After being diagnosed and a short time later having a mastectomy and all lymph nodes removed, chemo started just before Christmas and I am struggling with it! Ive got another 2 months of chemo before 5 weeks of Radiation…… would love to hear other stories. I have a fantastic support group of family, friends and colleagues but they just can’t possibly understand what I’m going through. Looking forward to connecting 😊
Hair Growing Back
Hi All, I am on my last paclitaxel chemo next week and staring to look beyond the chemo bad ass. I am just completing 8 courses of dose dense chemo - 4 xAC, 4x Paclitaxel and am wondering how long it took for others to grow their hair back. I know this is assuming it has grown back sufficiently, as some women are unlucky with hair regrowth. Just hoping you can share you experiences of when your hair grew back enough to actually feel like you had enough to do something with and any changes in your hair regrowth from before chemo. Many thanks, Jo
Liz O'Riordan - breast surgeon with BC Recommended to Read
I found this blog by an English breast surgeon who got BC herself to be incredibly useful & informative when I was first diagnosed. And then most especially the chemo guide when I found out I had to have it myself. She hasn't posted for a long time but a notification just popped into my inbox, she's writing again. So if you're into blogs, check it out. http://liz.oriordan.co.uk/MovingOn_files/this-is-who-I-am.html
Triple Negative
Hi there, I’m new to this site and to be honest very scared. I had surgery a week ago to have a cancer removed (lumpectomy). Results are in. Clear margins and clear nodes (that’s the good news) Grade 3 Stage 1 so caught an aggressive cancer early but I’m also triple negative. For the first time since my diagnosis my doctor used the word chemo and it scares me more than the initial diagnosis. Everything I read about triple negative is scary. Everything I read about Chemo is scary. It still needs to be discussed wether chemo will be beneficial for me. Has anyone been diagnosed with triple negative and not required Chemo?TC Chemotherapy
Had Round 3 of TC chemo on Monday morning. Bone aches arrived like clockwork on Thursday night, but now on Friday, I seem to have lower back pain and hip pain for the first time as well. Is this normal? I have been walking 1.5 - 2 kms each day this week. I am finding the variety, and variance, of side effects, to be weird. For example, Round 1, a little nausea, Round 2, a lot, Round 3, none so far.
Sick of the drainage!
Hi everyone, Please help with any advice 'seroma related' as I am very frustrated. My lump was removed start of December and I'm going tomorrow for my 7th drainage of the horrible '3rd boob' that is hanging out under my arm. My port and 1st chemo session were originally scheduled for 16th Jan but have now been postponed until 6th Feb! I know it's probably not a bad thing to delay on the 'poisoning' but I was ready to start and now I just feel in limbo. i have asked so many times if there is something I can do to stop the thing refilling ...compression, massage etc but everyone keeps saying that it will stop in its own time. Any advice is greatly appreciated as I just want to get rid of it! Thanks Kim x
Mum recently diagnosed
Hey all, I've joined this forum in the hopes of connecting with others. My mum is 69, diagnosed with breast cancer 2 months ago and now has been diagnosed with metastatic BC in spine and possibly lungs (they arent 100% sure on the lungs) as the spots are so small. Shes started oral chemo and hormone therapy today and will see the oncologist again in 5 weeks. She seems to be handling it well so far but she's not feeling sick or anything yet so i guess time will tell. Im sure its going to be a long journey and I'll be here to support her every step of the way. I currently live with my mum so im glad Im here to be there for her. I just wanted to pop in and say hi.Black nail polish for chemo
Hello all, I am about to have my 3rd round of TC in 2 days time. I noticed that 4 of my fingers have darken a bit. During the last 2 sessions, I did have my fingers painted with black nail polish. Would anyone know the main purpose of black nail polish, is it for blocking out UV rays during summer? Since it's winter now and I don't do out much, should I still continue painting my nails with black nail polish? Or is nail strengthener good enough? Thanks.
Reflux and shampoo for Cold Cap Chemo
I was diagnosed with early stage breast cancer with lumpectomy in October but I'm having four treatments of cold cap chemo AC and was wondering whether the Nioxin shampoo was a good one to use while going through this? Also what's the best for Reflux? This is my first post, so thanks for reading. Cheers.
Trodelvy - any info to share?
Hi, I am reaching out to see if anyone else has commenced Trodelvy chemotherapy and if yes, what are your side effects experiences. I am only in 1st cycle, 2 weeks on/1 week off. Main reaction has been some insomnia and bad fatigue. Wondering about hair loss and at what stage, if anyone has experienced this? Does fatigue get worse? Any other lurking side effects to be aware of?